Abstract

Commercial resin microbeads are widely applied in ion exchange and extraction. Here, a single anion-selective and phosphate binding resin microbead (FerrIX™) is mounted into an epoxy membrane and investigated by 4-electrode membrane voltammetry and membrane impedance spectroscopy. Anion transport properties are observed to dominate associated with three distinct potential domains: (I) a low bias ohmic potential domain (dominant at high electrolyte concentration), (II) a concentration polarisation potential domain, and (III) an over-limiting potential domain. Voltammetric responses show transient diffusion-migration features at higher scan rates and quasi-steady state features at lower scan rates. Inherent microbead conductivity is shown to be linked to two resistive elements, electrolyte concentration dependent and independent, in series. The effects of phosphate binding are revealed as transient pattern in impedance spectroscopy data. Preliminary data suggest phosphate concentration-dependent peak features in the imaginary impedance versus frequency plot due to phosphate binding into the microbead. Graphical abstract: [Figure not available: see fulltext.].

Original languageEnglish
Pages (from-to)2881-2891
Number of pages11
JournalJournal of Solid State Electrochemistry
Volume25
Issue number12
Early online date8 Jun 2021
DOIs
Publication statusPublished - 31 Dec 2021

Bibliographical note

Funding Information:
F.M. received support from the Leverhulme Foundation (RPG-2014–308: “New Materials for Ionic Diodes and Ionic Photodiodes”). A.K.T. received support from the Centre for Sustainable Chemical Technologies (CSCT) and the Engineering and Physical Sciences Research Council (EPSRC). K.M. received financial support from Provincie Gelderland. This work was supported by the Engineering and Physical Sciences Research Council EP/L016354/1.

Keywords

  • Desalination
  • Ion exchange
  • Ion selectivity
  • Pore resistivity
  • Transport

ASJC Scopus subject areas

  • General Materials Science
  • Condensed Matter Physics
  • Electrochemistry
  • Electrical and Electronic Engineering

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